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Triethylamine → HCID 39235298、化合物

HRID 1984466
ノート
印刷プレビュー

反応式

HRID 1984466 の反応式
C(N(CC)CC)C.[OH:8][CH2:9][CH2:10][N:11]1[C:15]([CH3:16])=[CH:14][C:13]([C:17]([NH2:19])=O)=[N:12]1.FC(F)(F)C(OC(=O)C(F)(F)F)=O>ClCCl>[OH:8][CH2:9][CH2:10][N:11]1[C:15]([CH3:16])=[CH:14][C:13]([C:17]#[N:19])=[N:12]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8471Triethylamine2 回HCID 9845Trifluoroacetic anhydride2 回HCID 669590521-(2-hydroxyethyl)-5-methyl-1H-pyrazole-3-carboxamide

生成物 1

HCID 39235298HCID 39235298、化合物収率 183.8%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

Under a nitrogen atmosphere, triethylamine (17.9 g, 177 mmol) was added to a slurry of 1-(2-hydroxyethyl)-5-methyl-1H-pyrazole-3-carboxamide (7.0 g, 41.4 mmol) in dichloromethane (70 mL). The mixture was cooled in an ice bath and then a solution of trifluoroacetic anhydride (15.6 g, 74.2 mmol) in dichloromethane (70 mL) was added over a period of 10 minutes. All of the solids dissolved to provide a cloudy solution. After 1 hour additional triethylamine (70.6 mmol) was added and the reaction mixture was cooled in an ice bath. Trifluoroacetic anhydride (35.3 mmol) was added neat over a period of 5 minutes. The reaction mixture was stirred for 10 minutes then the ice bath was removed and the reaction mixture was stirred for 30 minutes. The reaction mixture was diluted with 2 M aqueous sodium carbonate (100 mL) and water (100 mL) then extracted with chloroform (×3). The extracts were combined, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to provide 11.5 g of 1-(2-hydroxyethyl)-5-methyl-1H-pyrazole-3-carbonitrile a brown oil.

後処理

  1. temperatureThe mixture was cooled in an ice bath
  2. dissolutionAll of the solids dissolved
  3. customto provide a cloudy solution
  4. temperaturethe reaction mixture was cooled in an ice bath
  5. customthe ice bath was removed
  6. stirringthe reaction mixture was stirred for 30 minutes
  7. additionThe reaction mixture was diluted with 2 M aqueous sodium carbonate (100 mL) and water (100 mL)
  8. extractionthen extracted with chloroform (×3)
  9. dry with materialdried over magnesium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-ffa926481bcf4429b781f830fa92e0ab
出典データセット
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07544697B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート